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²éѯ½á¹û£º¹²²éµ½3718¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 2-deoxy-3-epi-4¦Â,20-dihydroxyecdysone ÏàËÆ¶È:92.3% Russian Chemical Bulletin 2000 49 1923-1924 A new phytoecdysteroid V. N. Odinokov, I. V. Galyautdinov, A. A. Fatykhov and L. M. Khalilov Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1¦Á,20R-hydroxyecdysone ÏàËÆ¶È:81.4% Natural Product Research and Development 2002 14(1) 9-12 STUDY ON THE CHEMICAL CONSTITUENTS OF LYCHNIS CORONARIA DAI Hao-fu; LIU Yu-qing; DENG Shi-ming; TAN Ning-hua; ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 20-hydroxyecdysone ÏàËÆ¶È:81.4% Food Chemistry 2005 92 125-132 Nutritional and antinutritional composition of Kancolla seeds: an interesting and underexploited andine food plant Irene Dini, Gian Carlo Tenore, Antonio Dini Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2-È¥Ñõ¼×¿ÇçÞͪ ÏàËÆ¶È:81.4% Journal of Chinese Medicinal Materials 2010 33 1574-1576 Studies on the Chemical Constituents from the Roots of Tinospora sagittata var. yunnanensis(¢ò) HUANG Xiang-zhong, CHENG Chun-mei, YIN Yan, GUO Jun-ming, LIANG Hui, DAI Yun Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 20-hydroxyecdysone ÏàËÆ¶È:80.7% Steroids 2002 67 127-135 Photochemical transformation of 20-hydroxyecdysone: production of monomeric and dimeric ecdysteroid analogues Juraj Harmatha, Miloš Budĕš¨ªnsky, Karel Vok¨¢ĕ Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 20-hydroxyecdysone C27H44O7 ÏàËÆ¶È:80.7% Phytochemistry 1998 49 2109-2114 Ecdysteroid constituents of the mushroom Tapinella panuoides Karel Vok¨¢, Milo Budnsky, Juraj Harmath¦Á, Jitka Kohoutov¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 20-hydroxy-ecdysone ÏàËÆ¶È:80.7% Phytochemistry 1994 37 707-711 Ecdysteroids from the roots of Leuzea carthamoides Jaroslav P¨ªš, Miloš Bud¨§š¨ªnsky̌, Karel Vok¨¢č, V¨§ra Laudov¨¢, Juraj Harmatha Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 20-hydroxyecdysone ÏàËÆ¶È:80.7% Tetrahedron 1998 54 1657-1666 New ergostane type ecdysteroids from fungi. Ecdysteroid constituents of mushroom Paxillus atrotomentosus Karel Vok¨¢č, Miloš Bud¨§š¨ªnsky, Juraj Harmatha, Jaroslav P¨ªš Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 2'-hydroxyecdysone ÏàËÆ¶È:77.7% Phytochemistry 2003 1179-1184 Ecdysteroids and other constituents from Sida spinosa L. Faten M.M. Darwish, Manfred G. Reinecke Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . integristerone A ÏàËÆ¶È:77.7% Helvetica Chimica Acta 2009 92 753-761 Ecdysteroids from Silene viridiflora Andr¨¢s Simon, No¨¦mi T¨®th, G¨¢bor T¨®th, Zolt¨¢n Kele, Judit Groska, M¨¢ria B¨¢thori Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . integristerone A ÏàËÆ¶È:77.7% Steroids 2004 69 389-394 A new ecdysteroid with unique 9¦Â-OH and four other ecdysteroids from Silene italica ssp. nemoralis Andr¨¢s Simon, Zita Pongr¨¢cz, G¨¢bor T¨®th, Marianna M¨¢k, Imre M¨¢th¨¦, M¨¢ria B¨¢thori Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 20-Hydroxyecdysone ÏàËÆ¶È:77.7% Steroids 2008 73 502-514 Additional minor ecdysteroid components of Leuzea carthamoides Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 20-hydroxyecdysone ÏàËÆ¶È:77.7% China Journal of Chinese Materia Medica 2003 28 730-732 Studies on Chemical Constituents in Herb of Lamium maculatum L. var Kansuense DENG Yanru, HE Li, LI Weiqi, WANG Hanqing Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 20-hydroxyecdysone ÏàËÆ¶È:77.7% Phytochemistry 1997 44 513-521 Ecdysteroid xylosides from Limnanthes douglasii Satyajit D. Sarker, Jean-Pierre Girault, Ren¨¦ Lafont, Laurence N. Dinan Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦Â-ecdysone C27H44O7 ÏàËÆ¶È:77.7% Journal of Natural Medicines 2010 64 114-116 New naphthoquinone from the root of Lygodium japonicum (Thunb.) Sw. Lijuan Chen, Guogang Zhang, Jie He, Jin Guan and Chunyuan Pan, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ¦Â-ecdysone C27H44O7 ÏàËÆ¶È:77.7% Chinese Traditional and Herbal Drugs 2006 37 1304-1306 °Î¶¾É¢»¯Ñ§³É·ÖµÄÑо¿ Àîά·å;ËÎÆôʾ;Ïîΰ;ÑîÊçÃô Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . ¦Â-ecdysterone C27H44O7 ÏàËÆ¶È:77.7% Journal of China Pharmaceutical University 2006 37 487-490 Chemical constituents from Asparagus filicinus WU Jia-jun; WANG Hao; YE Wen-cai; ZUO Xiao-feng; ZHAO Shou-xun Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . ¦Â-ecdysterone C27H44O7 ÏàËÆ¶È:77.7% Asian Journal of Traditional Medicines 2006 1 7-10 Anti-tumor Constituents from Paris polyphylla Yu Wang , Wenyuan Gao , Xinqiao Liu , Yutong Zuo , Haixia Chen, and Hongquan Duan Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 2¦Â,3¦Â,14¦Á,20¦Â,22¦Á,25-hexahydroxy-5¦Â-cholest-7-en-6-one C27H44O7 ÏàËÆ¶È:77.7% Indian Journal of Chemistry 1995 34B 674-676 NMR studies of 20¦Â-hydroxyecdysone,a steroid;isolated from Tinospora cordifolia A shish K Pathak, Pawan K Agariwal, Dharam C Jain, Ram P Sharma & Oliver W Howarth Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Ecdysterone ÏàËÆ¶È:76.9% Journal of Natural Products 1995 Vol 58 264-268 4-Dehydroecdysterone, a New Ecdysteroid from the Zoanthid Parazoanthus sp. Philip A. Searle, Tadeusz F. Molinski Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 20-Hydroxyecdysone 2-acetate C29H46O8 ÏàËÆ¶È:75.8% Steroids 2008 73 502-514 Additional minor ecdysteroid components of Leuzea carthamoides Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 2-deoxy-20-hydroxyecdysone ÏàËÆ¶È:74.0% Helvetica Chimica Acta 2009 92 753-761 Ecdysteroids from Silene viridiflora Andr¨¢s Simon, No¨¦mi T¨®th, G¨¢bor T¨®th, Zolt¨¢n Kele, Judit Groska, M¨¢ria B¨¢thori Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 20-hydroxyecdysone ÏàËÆ¶È:74.0% Korean Journal of Pharmacognosy 1999 30(3) 335-339 Isolatin and Quantitative Determination of 20-Hydroxyecdysone from Achyranthis Radix Hwang, Ji-Hyun; Lee, Seung-Ho; Park, Jeong-Hill; Kang, Shin-Jung; Chang, Seung-Yeup; Lee, Kyong-Soon; Son, Kun-Ho Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . Ecdysterone ÏàËÆ¶È:74.0% Chemistry of Natural Compounds 2010 46 173-175 A new alloside from Neocheiropteris palmatopedata Ye-Gao Chen, Jian-Hong Yang, Yan Zhang and Ying Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 20¦Â-hydroxy-ecdysone ÏàËÆ¶È:74.0% Natural Product Research and Development 2005 17 125-127 Chemical Constituents of Tinospora craveniana LI Hong-bo; HU Jun; CHEN Jian-chao; QIU Ming-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . cholest-7-en-2¦Â,3¦Â,14¦Á,20¦Â,22¦Á,25-hexahydroxy-6-one C27H44O7 ÏàËÆ¶È:74.0% Acta Scientiarum Naturalium Universitatis Sunyatseni 2003 42(5) 51-53 Polyhydroxylated Sterols from the Soft Coral Sinularia depressa ZHANG Guang-wen, MA Xiang-quan, SU Jing-yu, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 20-hydroxyecdysone ÏàËÆ¶È:73.0% Phytochemistry 1997 46 103-105 24(241)[Z]-dehydroamarasterone B, a phytoecdysteroid from seeds of Leuzea carthamoides U. A. Baltayev, L. Dinan, J. -P. Girault, R. Lafont Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . ¦Â-ecdysterone ÏàËÆ¶È:73.0% Natural Product Research and Development 2003 15 93-97 ECDYSTEROIDS FROM THE STEMS OF DIPLOCLISIA GLAUCESCENS HUANG Xiao chun GUO Yue wei ZHOU Wen liang ZUO Jian ping WANG Zheng tao Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 3-Deoxy-1¦Â ,20-dihydroxyecdysone C27H44O7 ÏàËÆ¶È:70.3% Steroids 2002 67 555-558 3-Deoxy-1¦Â,20-dihydroxyecdysone from the leaves of Diploclisia glaucescens Lalith Jayasinghe, Champika P. Jayasooriya, Kiyoshi Oyama, Yoshinori Fujimoto Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . polypodine B ÏàËÆ¶È:70.3% China Journal of Chinese Materia Medica 2005 30 272-274 Studies on chemical constituents in herb of Lamium maculatum var. kansuense DENG Yanru, DING Lan, WU Shuixian, WANG Hanqing Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . polypodine B ÏàËÆ¶È:70.3% Phytochemistry 1994 37 707-711 Ecdysteroids from the roots of Leuzea carthamoides Jaroslav P¨ªš, Miloš Bud¨§š¨ªnsky̌, Karel Vok¨¢č, V¨§ra Laudov¨¢, Juraj Harmatha Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 20¦Â-hydroxy-ecdysone-2-O-¦Â-D-glucopyranoside ÏàËÆ¶È:70.3% Natural Product Research and Development 2005 17 125-127 Chemical Constituents of Tinospora craveniana LI Hong-bo; HU Jun; CHEN Jian-chao; QIU Ming-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . polypodingB ÏàËÆ¶È:70.3% Natural Product Research and Development 2002 14(1) 9-12 STUDY ON THE CHEMICAL CONSTITUENTS OF LYCHNIS CORONARIA DAI Hao-fu; LIU Yu-qing; DENG Shi-ming; TAN Ning-hua; ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . Inokosterone 20,22-acetonide C30H48O7 ÏàËÆ¶È:70% Steroids 2008 73 502-514 Additional minor ecdysteroid components of Leuzea carthamoides Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . 2-deoxyintegristerone A ÏàËÆ¶È:69.2% Helvetica Chimica Acta 2009 92 753-761 Ecdysteroids from Silene viridiflora Andr¨¢s Simon, No¨¦mi T¨®th, G¨¢bor T¨®th, Zolt¨¢n Kele, Judit Groska, M¨¢ria B¨¢thori Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . (20R,22R)-20,22-Dihydroxycholest-5-ene C27H46O3 ÏàËÆ¶È:69.2% Steroids 2008 73 1452-1464 Synthesis of ponasterone A derivatives with various steroid skeleton moieties and evaluation of their binding to the ecdysone receptor of Kc cells Hirokazu Arai, Bunta Watanabe, Yoshiaki Nakagawa, Hisashi Miyagawa Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . ponasterone A C27H44O6 ÏàËÆ¶È:69.2% Phytochemistry 1998 49 2109-2114 Ecdysteroid constituents of the mushroom Tapinella panuoides Karel Vok¨¢, Milo Budnsky, Juraj Harmath¦Á, Jitka Kohoutov¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . turkesterone C27H44O8 ÏàËÆ¶È:69.2% Phytochemistry 1998 49 2109-2114 Ecdysteroid constituents of the mushroom Tapinella panuoides Karel Vok¨¢, Milo Budnsky, Juraj Harmath¦Á, Jitka Kohoutov¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . ponasterone A ÏàËÆ¶È:69.2% Russian Journal of Organic Chemistry 2002 38 525-529 Ozonolysis of Alkenes and Study of Reactions of Polyfunctional Compounds: LXVI.2* Ozonolysis and Hydrogenation of Diacetonides of 24,25- and 25,26-Anhydro-20-hydroxyecdysones. Synthesis of Ponasterone A V. N. Odinokov, R. G. Savchenko, S. R. Nazmeeva, I. V. Galyautdinov and L. M. Khalilov Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . 11¦Â-hydroxy-20-deoxyshidasterone C27H42O6 ÏàËÆ¶È:69.2% Planta Medica 2013 79 52-59 Phytoecdysteroids from the Stem Bark of Vitex doniana and Their Anti-Inflammatory Effects Ochieng, Charles O.; Ishola, Ismail O.; Opiyo, Sylvia A.; Manguro, Lawrence A.O.; Owuor, Philip O.; Wong, Keng-Chong: Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . 20-hydroxyecdysone 2,3-monoacetonide ÏàËÆ¶È:68.9% Phytochemistry 1994 37 707-711 Ecdysteroids from the roots of Leuzea carthamoides Jaroslav P¨ªš, Miloš Bud¨§š¨ªnsky̌, Karel Vok¨¢č, V¨§ra Laudov¨¢, Juraj Harmatha Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . 24-epimakisterone A ÏàËÆ¶È:67.8% Chemistry & Biodiversity 2008 Vol. 5 707 Ecdysteroids from Vitex Species: Distribution and Compilation of Their 20C-NMR Spectral Data Jos¨¦ G. Sena Filho, Jennifer Duringer, Gabriela L. A. Maia, Josean F. Tavares, Haroudo S. Xavier, Marcelo Sobral da Silva, Em.dio V. L. da-Cunha, and Jos¨¦ M. Barbosa-Filho Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . 24-epi-makisterone A ÏàËÆ¶È:67.8% Planta Medica 1985 51 40-42 Phytoecdysteroids of Diploclisia glaucescens Seed R. W. Miller, J. C1ardy, J. Kozlowski, K. L. Mikolajczak, R. D. Plattner, R. G. Powell, C. R. Smith, D. Weisleder and Zheng Qi-Tai Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . 24-epi-makisterone A C28H46O7 ÏàËÆ¶È:67.8% Chinese Traditional and Herbal Drugs 2001 32 12-13 Isolation and identification of non alkaloid components from Tinospora hainanensis (¢ó) LIN Lian bo; FU Xiao wen; GUO You ying; Keisuke KOJIMA; Ykio OGIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . 24-Epi-makisterone A ÏàËÆ¶È:67.8% Journal of Agricultural and Food Chemistry 2001 49 2576-2578 Ecdysteroids of Quinoa Seeds (Chenopodium quinoa Willd.) Nanqun Zhu, Hiroe Kikuzaki, Bret C. Vastano, Nobuji Nakatani, Mukund V. Karwe, Robert T. Rosen, and Chi-Tang Ho Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . Polypodine B 2-¦Â-D-glucoside C33H54O13 ÏàËÆ¶È:67.7% Steroids 2011 76 1419-1424 Ecdysteroids from Polypodium vulgare L. Andr¨¢s Simon, Attila V¨¢nyol¨®s, Zolt¨¢n B¨¦ni, Mikl¨®s D¨¦k¨¢ny, G¨¢bor T¨®th, M¨¢ria B¨¢thori Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . (2¦Â,3¦Á,5¦Â,22R)-2,3,20,22,25-pentahydroxycholest- 7-en-6-one C27H44O6 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2008 Vol. 91 1640 Additional Minor Phytoecdysteroids of Serratula wolffii Andr¨¢s Simon, Erika Liktor-Busa, G¨¢bor To¡ä th, Zolt¨¢n Kele, Judit Groska, and M¨¢ria B¨¢thori¨® Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . ponasterone A ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2008 Vol. 91 1640 Additional Minor Phytoecdysteroids of Serratula wolffii Andr¨¢s Simon, Erika Liktor-Busa, G¨¢bor To¡ä th, Zolt¨¢n Kele, Judit Groska, and M¨¢ria B¨¢thori¨® Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 2¦Â,3¦Â,14¦Á,20¦Â,22¦Á,25¦Â-hexahydroxycholest-7-en-6-one ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 2007 43 672-677 SEPARATION AND IDENTIFICATION OF STEROIDAL COMPOUNDS WITH CYTOTOXIC ACTIVITY AGAINST HUMAN GASTRIC CANCER CELL LINES IN VITRO FROM THE RHIZOMES OF Paris polyphylla VAR. chinensis Huang Yun, Cui Lijian, Zhan Wenhong Dou Yuhong,Wang Yongli, Wang Qiang, and Zhao Ding Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . Sileneoside D ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 1998 34 602-604 PItYTOECDYSTEROIDS OF PLANTS OF THE Silene GENUS. XIX. THE STRUCTURE OF SILENEOSIDE G Z. T. Sadykov and Z. Saatov Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . 2-deoxyecdysterone ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 1985 21 56-58 PHYTOECDYSTEROIDS OF PLANTS OF THE GENUS Silene.VIII. 2-DEOXYECDYSTERONE 3-ACETATE FROM Silene pvaemixta Z. Saatov, M. B. Gorovits,N. D. Abdullaev, B. Z. Usmanov, and N. K. Abubakirov Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . 20,26-dihydroxyecdysone ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2009 92 753-761 Ecdysteroids from Silene viridiflora Andr¨¢s Simon, No¨¦mi T¨®th, G¨¢bor T¨®th, Zolt¨¢n Kele, Judit Groska, M¨¢ria B¨¢thori Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . ecdysterone ÏàËÆ¶È:66.6% Acta Botanica Sinica 1996 38 399-405 Studieson the Chemical Constituents of the Leaves of Pseudotaxus chienii (Cheng)Cheng Zhang Jun-zeng, Fang Qi-cheng and Liang Xiao-tian Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . 22-deoxyecdysterone ÏàËÆ¶È:66.6% Acta Botanica Sinica 2001 43 316-318 Phytoecdysterones from Cucubalus baccifer CHENG Yong-Xian, ZHOU Jun, TAN Ning-Hua, DING Zhong-Tao Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . 9¦Â,20-Dihydroxyecdysone C27H45O8 ÏàËÆ¶È:66.6% Steroids 2004 69 389-394 A new ecdysteroid with unique 9¦Â-OH and four other ecdysteroids from Silene italica ssp. nemoralis Andr¨¢s Simon, Zita Pongr¨¢cz, G¨¢bor T¨®th, Marianna M¨¢k, Imre M¨¢th¨¦, M¨¢ria B¨¢thori Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . 22-Deoxy-integristerone A ÏàËÆ¶È:66.6% Steroids 2004 69 389-394 A new ecdysteroid with unique 9¦Â-OH and four other ecdysteroids from Silene italica ssp. nemoralis Andr¨¢s Simon, Zita Pongr¨¢cz, G¨¢bor T¨®th, Marianna M¨¢k, Imre M¨¢th¨¦, M¨¢ria B¨¢thori Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . (20R,22R)-Cholest-5-ene-3¦Â,20,22-triol C27H46O3 ÏàËÆ¶È:66.6% Steroids 2004 69 483-493 Stereoselective synthesis of (22R)- and (22S)-castasterone/ponasterone A hybrid compounds and evaluation of their molting hormone activity Bunta Watanabe, Yoshiaki Nakagawa, Takehiko Ogura, Hisashi Miyagawa Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . Ajugasterone C ÏàËÆ¶È:66.6% Steroids 2008 73 502-514 Additional minor ecdysteroid components of Leuzea carthamoides Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka Structure 13C NMR ̼Æ×Ä£Äâͼ 59 . ponasterone A ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2007 32 1421-1425 Non-taxoid chemical constituents from leaves of Taxus mairei ZHANG Manli, HUO Changhong, DONG Mei, LIANG Chunhui, GU Yucheng, SHI Qingwen Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . 25-hydroxypanuosterone C28H46O8 ÏàËÆ¶È:66.6% Phytochemistry 1998 49 2109-2114 Ecdysteroid constituents of the mushroom Tapinella panuoides Karel Vok¨¢, Milo Budnsky, Juraj Harmath¦Á, Jitka Kohoutov¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 61 . ¦Â-ecdysone C27H44O7 ÏàËÆ¶È:66.6% Acta Pharmaceutica Sinica 1990 Vol 25 509-514 STEROIDAL SAPONINS FROM ASPARAGUS FILICINUS Y Ding and CR Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 62 . 1-hydroxy-22-deoxy-20,21-didehydro-ecdysone C27H42O6 ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 2010 48 386-391 Structure and stereochemistry of novel ecdysteroids from the roots of Serratula wolffii (pages 386¨C391) M¨¢ria Tak¨¢cs, Andr¨¢s Simon, Erika Liktor-Busa, M¨¢ria B¨¢thori, Ferenc Zsila, Zsolt Bik¨¢di, P¨¦ter Horv¨¢th, G¨¢bor Veress, Andr¨¢s Gergely and G¨¢bor T¨®th Structure 13C NMR ̼Æ×Ä£Äâͼ 63 . (20R,22R)-Cholest-5-ene-3¦Â,20,22-triol ÏàËÆ¶È:66.6% Steroids 1999 64 385-395 An improved synthesis of(20R,22R)-cholest-5-ene-3¦Â,20,22-triol, an intermediate in steroid hormone formation and an activator of nuclear orphan receptor LXR¦Á Benfang Ruan, William K. Wilson, George J. SchroepferJr. Structure 13C NMR ̼Æ×Ä£Äâͼ 64 . 25-hydroxycholestero ÏàËÆ¶È:66.6% Steroids 1994 59 310-317 Inhibitors of sterol synthesis. Effects of fluorine substitution at carbon atom 25 of cholesterol on its spectral and chromatographic properties and on 3-hydroxy-3-methylglutaryl coenzyme a reductase activity in CHO-K1 cells William K. Wilson, Shankar Swaminathan, Frederick D. Pinkerton, Nicolas Gerst, George J. Schroepfer Jr. Structure 13C NMR ̼Æ×Ä£Äâͼ 65 . Ë®Áú¹ÇËØ B C27H44O8 ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 2006 37 1304-1306 °Î¶¾É¢»¯Ñ§³É·ÖµÄÑо¿ Àîά·å;ËÎÆôʾ;Ïîΰ;ÑîÊçÃô Structure 13C NMR ̼Æ×Ä£Äâͼ 66 . ponasterone A ÏàËÆ¶È:66.6% Chinese Journal of Medicinal Chemistry 2006 16 46-48 Isolation and identification of the chemical constituents from Mangrove plant Acrostichum a ureurm MEI Wen-li, ZENG Yan-bo, DING Zhong-tao, DAI Hao-fu Structure 13C NMR ̼Æ×Ä£Äâͼ 67 . paristerone ÏàËÆ¶È:66.6% Natural Product Research and Development 2003 15 93-97 ECDYSTEROIDS FROM THE STEMS OF DIPLOCLISIA GLAUCESCENS HUANG Xiao chun GUO Yue wei ZHOU Wen liang ZUO Jian ping WANG Zheng tao Structure 13C NMR ̼Æ×Ä£Äâͼ 68 . 20-hydroxyecdysone (6E)-oxime C27H45NO7 ÏàËÆ¶È:66.6% Russian Journal of Organic Chemistry 2006 42 1333-1339 Synthesis of 20-hydroxyecdysone oxime, its diacetonide, and their 14,15-anhydro derivatives I. V. Galyautdinov, N. A. Ves¡¯kina, S. R. Afon¡¯kina, L. M. Khalilov and V. N. Odinokov Structure 13C NMR ̼Æ×Ä£Äâͼ 69 . Ë®Áú¹ÇçÞͪ B C27H44O8 ÏàËÆ¶È:66.6% Journal of Tropical and Subtropical Botany 2010 18 569-572 Chemical Constituents from Seeds of Achyranthes bidentata Blume. DONG, Qinqin, YAN, Jian, ZHENG, Mengfei, HUAI, Huyin, TAN, Jianwen Structure 13C NMR ̼Æ×Ä£Äâͼ 70 . dyscusin A C29H50O4 ÏàËÆ¶È:65.5% Chemical & Pharmaceutical Bulletin 2011 59(10) 1303-1306 Dyscusins A-C, Three New Steroids from the Leaves of Dysoxylum cumingianum Shin-ichiro KURIMOTO, Yoshiki KASHIWADA, Susan Lynne MORRIS-NATSCHKE, Kuo-Hsiung LEE, and Yoshihisa TAKAISHI Structure 13C NMR ̼Æ×Ä£Äâͼ 71 . 1¦Á,20¦Á-dihydroxyecdysone ÏàËÆ¶È:65.3% Journal of Natural Products 2002 65 1194-1197 Ecdysteroids from a Zoanthus sp. Apichart Suksamrarn,Aroon Jankam, Bongkoch Tarnchompoo, and Sumaitt Putchakarn Structure 13C NMR ̼Æ×Ä£Äâͼ 72 . 2-deoxyecdysterone C27H44O6 ÏàËÆ¶È:65.3% Acta Botanica Yunnanica 2000 22(3) 351-357 Phytoecdysones from Porana discifera ZHU Wei-Ming,YANG Xiao-Sheng,HE Hong-Ping,HAO Xiao-Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 73 . 20-hydroxyecdysone C27H44O7 ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 1990 38 1927-1930 The Constituents of Cistanche tubulosa (SCHRENK) HOOK. f. II. : Isolation and Structures of a New Phenylethanoid Glycoside and a New Neolignan Glycoside Fumio YOSHIZAWA,Takeshi DEYAMA,Nobuo TAKIZAWA,Khan USMANGHANI and Mansoor AHMAD Structure 13C NMR ̼Æ×Ä£Äâͼ 74 . 3¦Â-Hydroxy-23,24-bisnornorchol-5-en-22-carbaldehyde ÏàËÆ¶È:65.3% Steroids 2005 70 551-562 Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Natalya B. Khripach, Alexey V. Antonchick, Andrey P. Antonchick, Bernd Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ 75 . (3¦Á,8¦Á,9¦Â,10¦Á,13¦Á,14¦Â,17¦Á,20S)-25-Hydroxycholesterol C27H46O2 ÏàËÆ¶È:65.3% Steroids 2006 71 484-488 Synthesis of ent-25-hydroxycholesterol Emily J. Westover, Douglas F. Covey Structure 13C NMR ̼Æ×Ä£Äâͼ 76 . 3¦Â ,25-dihydroxy-5-ene C27H46O2 ÏàËÆ¶È:65.3% Steroids 2009 74 81-87 A facile synthesis of C-24 and C-25 oxysterols by in situ generated ethyl(trifluoromethyl)dioxirane Shoujiro Ogawa, Genta Kakiyama, Akina Muto, Atsuko Hosoda, Kuniko Mitamura, Shigeo Ikegawa, Alan F. Hofmann, Takashi Iida Structure 13C NMR ̼Æ×Ä£Äâͼ 77 . 1¦Á,20R-dihydroxyecdysone C38H44O8 ÏàËÆ¶È:65.3% Phytochemistry 1998 49 2305-2310 1¦Á,20R-Dihydroxyecdysone from axyris amaranthoides Satyajit D. Sarker, Vladimir Sik, Huw H. Rees, Laurence Dinan Structure 13C NMR ̼Æ×Ä£Äâͼ 78 . 16-O-acetylgitoxigenin ÏàËÆ¶È:65.3% Chinese Pharmaceutical Journal 2007 42 420-422 Studies on Chemical Constituents of Streptocaulon griffithii ZHANG Lin, WANG Ye-fei, XU Li-zhen Structure 13C NMR ̼Æ×Ä£Äâͼ 79 . makisterone A ÏàËÆ¶È:64.2% Chemistry & Biodiversity 2008 Vol. 5 707 Ecdysteroids from Vitex Species: Distribution and Compilation of Their 36C-NMR Spectral Data Jos¨¦ G. Sena Filho, Jennifer Duringer, Gabriela L. A. Maia, Josean F. Tavares, Haroudo S. Xavier, Marcelo Sobral da Silva, Em.dio V. L. da-Cunha, and Jos¨¦ M. Barbosa-Filho Structure 13C NMR ̼Æ×Ä£Äâͼ 80 . makisterone A ÏàËÆ¶È:64.2% Planta Medica 1985 51 40-42 Phytoecdysteroids of Diploclisia glaucescens Seed R. W. Miller, J. C1ardy, J. Kozlowski, K. L. Mikolajczak, R. D. Plattner, R. G. Powell, C. R. Smith, D. Weisleder and Zheng Qi-Tai Structure 13C NMR ̼Æ×Ä£Äâͼ 81 . (3¦Â,23R)-ergost¦Á-5,24(28)-diene-3,23-diol C28H46O2 ÏàËÆ¶È:64.2% Chemistry & Biodiversity 2009 6 86-95 Revision of the Absolute Configuration at C(23) of Lanostanoids and Isolation of Secondary Metabolites from Formosan Soft Coral Nephthea erecta Shi-Yie Cheng, Zhi-Hong Wen, Shang-Kewi Wang, Michael Y. Chiang, Ali A. H. El-Gamal, Chang-Feng Dai, and Chang-Yih Duh Structure 13C NMR ̼Æ×Ä£Äâͼ 82 . Makisterone A C28H46O7 ÏàËÆ¶È:64.2% Chemistry of Natural Compounds 1999 35 184-185 RI-IAPISTERONE D 20-ACETATE FROM THE SEEDS OF Leuzea carthamoides E. B. Borovikova, G. S. Shangaraeva,and U. A. Baltaev Structure 13C NMR ̼Æ×Ä£Äâͼ 83 . 24-epi-Makisterone A ÏàËÆ¶È:64.2% Steroids 2008 73 502-514 Additional minor ecdysteroid components of Leuzea carthamoides Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka Structure 13C NMR ̼Æ×Ä£Äâͼ 84 . ergosta-5,24(24')-diene-3¦Â,4¦Â,20S-triol C28H46O3 ÏàËÆ¶È:64.2% Phytochemistry 1997 44 153-155 Ergosta-5, 24(24')-diene-3¦Â, 4¦Â, 20S-triol, an ergostane steroid from Dysoxylum malabaricum T. R. Govindachari, G. N. Krishna Kumari, G. Suresh Structure 13C NMR ̼Æ×Ä£Äâͼ 85 . makisterone A ÏàËÆ¶È:64.2% Korean Journal of Pharmacognosy 1998 29(4) 318-322 Studies on the Constituents from the Herbs of Ajuga multiflora (II) Yu, Young-Jun; Do, Jae-Chul; Kwon, Soon-Youl; Son, Kun-Ho Structure 13C NMR ̼Æ×Ä£Äâͼ 86 . 22E,24R-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â,9¦Á-tetraol C28H46O4 ÏàËÆ¶È:64.2% Chinese Journal of Medicinal Chemistry 2008 18 279-283 Chemical constituents from endophytic fungus S26 of Cephalotaxus hainanensis CHEN Ping, WU Jiao, DAI Hao-fu, XIE Xiu-chao, MEI Wen-li Structure 13C NMR ̼Æ×Ä£Äâͼ 87 . (22E,24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Á,9¦Á-tetraol C32H52O4 ÏàËÆ¶È:64.2% Natural Product Research and Development 2007 19 436-438 Chemical Constituents of Basidiomycetes Russula subnigricans GONG Qing-fang; ZHANG Yu-mei; TAN Ning-hua; CHEN Zuo-hong Structure 13C NMR ̼Æ×Ä£Äâͼ 88 . 20-hydroxyecdysone 2-mesylate C28H46O9S ÏàËÆ¶È:64.2% Tetrahedron 2008 64 2626-2633 Functional group-mediated biotransformation by Curvularia lunata NRRL 2178: synthesis of 3-dehydro-2-deoxy-ecdysteroids from the 3-hydroxy-2-mesyloxy analogues Chatchawan Changtam, Oratai Sukcharoen, Boon-ek Yingyongnarongkul, Nitirat Chimnoi, Apichart Suksamrarn Structure 13C NMR ̼Æ×Ä£Äâͼ 89 . Makisterone A ÏàËÆ¶È:64.2% Journal of Agricultural and Food Chemistry 2001 49 2576-2578 Ecdysteroids of Quinoa Seeds (Chenopodium quinoa Willd.) Nanqun Zhu, Hiroe Kikuzaki, Bret C. Vastano, Nobuji Nakatani, Mukund V. Karwe, Robert T. Rosen, and Chi-Tang Ho Structure 13C NMR ̼Æ×Ä£Äâͼ 90 . 2, 3-acetonide ¦Â-ecdysterone C30H48O7 ÏàËÆ¶È:63.3% Acta Botanica Yunnanica 2000 22(3) 351-357 Phytoecdysones from Porana discifera ZHU Wei-Ming,YANG Xiao-Sheng,HE Hong-Ping,HAO Xiao-Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 91 . Integristeone A ÏàËÆ¶È:63.3% Steroids 2008 73 502-514 Additional minor ecdysteroid components of Leuzea carthamoides Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka Structure 13C NMR ̼Æ×Ä£Äâͼ 92 . limnantheoside B C32H52O10 ÏàËÆ¶È:63.3% Phytochemistry 1997 44 513-521 Ecdysteroid xylosides from Limnanthes douglasii Satyajit D. Sarker, Jean-Pierre Girault, Ren¨¦ Lafont, Laurence N. Dinan Structure 13C NMR ̼Æ×Ä£Äâͼ 93 . 20-hydroxyecdysone ÏàËÆ¶È:62.9% Chemistry & Biodiversity 2008 Vol. 5 707 Ecdysteroids from Vitex Species: Distribution and Compilation of Their 13C-NMR Spectral Data Jos¨¦ G. Sena Filho, Jennifer Duringer, Gabriela L. A. Maia, Josean F. Tavares, Haroudo S. Xavier, Marcelo Sobral da Silva, Em.dio V. L. da-Cunha, and Jos¨¦ M. Barbosa-Filho Structure 13C NMR ̼Æ×Ä£Äâͼ 94 . Shidasterone ÏàËÆ¶È:62.9% Chemistry & Biodiversity 2008 Vol. 5 707 Ecdysteroids from Vitex Species: Distribution and Compilation of Their 17C-NMR Spectral Data Jos¨¦ G. Sena Filho, Jennifer Duringer, Gabriela L. A. Maia, Josean F. Tavares, Haroudo S. Xavier, Marcelo Sobral da Silva, Em.dio V. L. da-Cunha, and Jos¨¦ M. Barbosa-Filho Structure 13C NMR ̼Æ×Ä£Äâͼ 95 . eurysterol A C27H45O7SNa ÏàËÆ¶È:62.9% Journal of Natural Products 2007 70 846-848 Eurysterols A and B, Cytotoxic and Antifungal Steroidal Sulfates from a Marine Sponge of the Genus Euryspongia Chollaratt Boonlarppradab* and D. John Faulkner Structure 13C NMR ̼Æ×Ä£Äâͼ 96 . eurysterol B C27H43O7SNa ÏàËÆ¶È:62.9% Journal of Natural Products 2007 70 846-848 Eurysterols A and B, Cytotoxic and Antifungal Steroidal Sulfates from a Marine Sponge of the Genus Euryspongia Chollaratt Boonlarppradab* and D. John Faulkner Structure 13C NMR ̼Æ×Ä£Äâͼ 97 . 20-hydroxyecdysone ÏàËÆ¶È:62.9% Journal of Natural Products 2002 65 1194-1197 Ecdysteroids from a Zoanthus sp. Apichart Suksamrarn,Aroon Jankam, Bongkoch Tarnchompoo, and Sumaitt Putchakarn Structure 13C NMR ̼Æ×Ä£Äâͼ 98 . 20-hydroxyecdysone ÏàËÆ¶È:62.9% Journal of Natural Products 2002 65 1690-1692 Ecdysteroids of Vitex scabra Stem Bark Apichart Suksamrarn, Saowanee Kumpun, and Boon-ek Yingyongnarongkul Structure 13C NMR ̼Æ×Ä£Äâͼ 99 . ¦Â-ecdysone C27H44O7 ÏàËÆ¶È:62.9% Acta Botanica Yunnanica 2000 22(4) 503-506 Phytoecdysones from Sida szechuensis YAO Chun-Suo,XU Yun-Long Structure 13C NMR ̼Æ×Ä£Äâͼ 100 . dcdysterone ÏàËÆ¶È:62.9% Chemical & Pharmaceutical Bulletin 1994 42 1116-1122 Three New Furostanol Saponins from the Bulbs of Ipheion uniflorum Osamu NAKAMURA,Yoshihiro MIMAKI,Yutaka SASHIDA,Tamotsu NIKAIDO and Taichi OHMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ |
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²éѯ½á¹û£º¹²²éµ½3718¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 2-deoxy-3-epi-4¦Â,20-dihydroxyecdysone ÏàËÆ¶È:92.3% Russian Chemical Bulletin 2000 49 1923-1924 A new phytoecdysteroid V. N. Odinokov, I. V. Galyautdinov, A. A. Fatykhov and L. M. Khalilov Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1¦Á,20R-hydroxyecdysone ÏàËÆ¶È:81.4% Natural Product Research and Development 2002 14(1) 9-12 STUDY ON THE CHEMICAL CONSTITUENTS OF LYCHNIS CORONARIA DAI Hao-fu; LIU Yu-qing; DENG Shi-ming; TAN Ning-hua; ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 20-hydroxyecdysone ÏàËÆ¶È:81.4% Food Chemistry 2005 92 125-132 Nutritional and antinutritional composition of Kancolla seeds: an interesting and underexploited andine food plant Irene Dini, Gian Carlo Tenore, Antonio Dini Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2-È¥Ñõ¼×¿ÇçÞͪ ÏàËÆ¶È:81.4% Journal of Chinese Medicinal Materials 2010 33 1574-1576 Studies on the Chemical Constituents from the Roots of Tinospora sagittata var. yunnanensis(¢ò) HUANG Xiang-zhong, CHENG Chun-mei, YIN Yan, GUO Jun-ming, LIANG Hui, DAI Yun Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 20-hydroxyecdysone ÏàËÆ¶È:80.7% Steroids 2002 67 127-135 Photochemical transformation of 20-hydroxyecdysone: production of monomeric and dimeric ecdysteroid analogues Juraj Harmatha, Miloš Budĕš¨ªnsky, Karel Vok¨¢ĕ Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 20-hydroxyecdysone C27H44O7 ÏàËÆ¶È:80.7% Phytochemistry 1998 49 2109-2114 Ecdysteroid constituents of the mushroom Tapinella panuoides Karel Vok¨¢, Milo Budnsky, Juraj Harmath¦Á, Jitka Kohoutov¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 20-hydroxy-ecdysone ÏàËÆ¶È:80.7% Phytochemistry 1994 37 707-711 Ecdysteroids from the roots of Leuzea carthamoides Jaroslav P¨ªš, Miloš Bud¨§š¨ªnsky̌, Karel Vok¨¢č, V¨§ra Laudov¨¢, Juraj Harmatha Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 20-hydroxyecdysone ÏàËÆ¶È:80.7% Tetrahedron 1998 54 1657-1666 New ergostane type ecdysteroids from fungi. Ecdysteroid constituents of mushroom Paxillus atrotomentosus Karel Vok¨¢č, Miloš Bud¨§š¨ªnsky, Juraj Harmatha, Jaroslav P¨ªš Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 2'-hydroxyecdysone ÏàËÆ¶È:77.7% Phytochemistry 2003 1179-1184 Ecdysteroids and other constituents from Sida spinosa L. Faten M.M. Darwish, Manfred G. Reinecke Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . integristerone A ÏàËÆ¶È:77.7% Helvetica Chimica Acta 2009 92 753-761 Ecdysteroids from Silene viridiflora Andr¨¢s Simon, No¨¦mi T¨®th, G¨¢bor T¨®th, Zolt¨¢n Kele, Judit Groska, M¨¢ria B¨¢thori Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . integristerone A ÏàËÆ¶È:77.7% Steroids 2004 69 389-394 A new ecdysteroid with unique 9¦Â-OH and four other ecdysteroids from Silene italica ssp. nemoralis Andr¨¢s Simon, Zita Pongr¨¢cz, G¨¢bor T¨®th, Marianna M¨¢k, Imre M¨¢th¨¦, M¨¢ria B¨¢thori Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 20-Hydroxyecdysone ÏàËÆ¶È:77.7% Steroids 2008 73 502-514 Additional minor ecdysteroid components of Leuzea carthamoides Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 20-hydroxyecdysone ÏàËÆ¶È:77.7% China Journal of Chinese Materia Medica 2003 28 730-732 Studies on Chemical Constituents in Herb of Lamium maculatum L. var Kansuense DENG Yanru, HE Li, LI Weiqi, WANG Hanqing Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 20-hydroxyecdysone ÏàËÆ¶È:77.7% Phytochemistry 1997 44 513-521 Ecdysteroid xylosides from Limnanthes douglasii Satyajit D. Sarker, Jean-Pierre Girault, Ren¨¦ Lafont, Laurence N. Dinan Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦Â-ecdysone C27H44O7 ÏàËÆ¶È:77.7% Journal of Natural Medicines 2010 64 114-116 New naphthoquinone from the root of Lygodium japonicum (Thunb.) Sw. Lijuan Chen, Guogang Zhang, Jie He, Jin Guan and Chunyuan Pan, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ¦Â-ecdysone C27H44O7 ÏàËÆ¶È:77.7% Chinese Traditional and Herbal Drugs 2006 37 1304-1306 °Î¶¾É¢»¯Ñ§³É·ÖµÄÑо¿ Àîά·å;ËÎÆôʾ;Ïîΰ;ÑîÊçÃô Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . ¦Â-ecdysterone C27H44O7 ÏàËÆ¶È:77.7% Journal of China Pharmaceutical University 2006 37 487-490 Chemical constituents from Asparagus filicinus WU Jia-jun; WANG Hao; YE Wen-cai; ZUO Xiao-feng; ZHAO Shou-xun Structure 13C NMR ̼Æ×Ä£Äâͼ |

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